119-61-9
Chemical Structure
Benzophenone
- CAS No.: 119-61-9
- Formula:C13H10O
- Molecular Weight:182.22
IUPAC Name: benzophenone
InChIKey: RWCCWEUUXYIKHB-UHFFFAOYSA-N
SMILES: O=C(C1=CC=CC=C1)C2=CC=CC=C2
Biological Activity: Benzophenone is an endogenous metabolite. Benzophenone is a photosensitizer, that absorbs UV light, transfers its energy to DNA, and triggers DNA damage. Benzophenone can be used as the fragrance enhancer, ultraviolet curing agent, additive in plastics, or the flavor ingredient. Benzophenone can also be used in the manufacturing of insecticides, agricultural chemicals, hypnotics, antihistamines, and other pharmaceuticals. Benzophenone exhibits certain carcinogenicity in mouse/rat models under long term exposure. Benzophenone exhibits estrogenic activity[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
Benzophenone | 99.99% | Benzophenone is an endogenous metabolite. Benzophenone is a photosensitizer, that absorbs UV light, transfers its energy to DNA, and triggers DNA damage. Benzophenone can be used as the fragrance enhancer, ultraviolet curing agent, additive in plastics, or the flavor ingredient. Benzophenone can also be used in the manufacturing of insecticides, agricultural chemicals, hypnotics, antihistamines, and other pharmaceuticals. Benzophenone exhibits certain carcinogenicity in mouse/rat models under long term exposure. Benzophenone exhibits estrogenic activity. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Benzophenone (Standard) | ≥98% | Benzophenone (Standard) is the analytical standard of Benzophenone. This product is intended for research and analytical applications. Benzophenone standard is a photosensitizer, that absorbs UV light, transfers its energy to DNA, and triggers DNA damage. Benzophenone standard can be used as the fragrance enhancer, ultraviolet curing agent, additive in plastics, or the flavor ingredient. Benzophenone standard can also be used in the manufacturing of insecticides, agricultural chemicals, hypnotics, antihistamines, and other pharmaceuticals. Benzophenone standard exhibits certain carcinogenicity in mouse/rat models under long term exposure. Benzophenone standard exhibits estrogenic activity. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Benzophenone-13C | 99.80% | Benzophenone-13C is the 13C labeled Benzophenone (HY-Y0546). Benzophenone is an endogenous metabolite. Benzophenone is a photosensitizer, that absorbs UV light, transfers its energy to DNA, and triggers DNA damage. Benzophenone can be used as the fragrance enhancer, ultraviolet curing agent, additive in plastics, or the flavor ingredient. Benzophenone can also be used in the manufacturing of insecticides, agricultural chemicals, hypnotics, antihistamines, and other pharmaceuticals. Benzophenone exhibits certain carcinogenicity in mouse/rat models under long term exposure. Benzophenone exhibits estrogenic activity. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Benzophenone-d5 | 99.98% | Benzophenone-d5 is the deuterium labeled Benzophenone (HY-Y0546). Benzophenone is an endogenous metabolite. Benzophenone is a photosensitizer, that absorbs UV light, transfers its energy to DNA, and triggers DNA damage. Benzophenone can be used as the fragrance enhancer, ultraviolet curing agent, additive in plastics, or the flavor ingredient. Benzophenone can also be used in the manufacturing of insecticides, agricultural chemicals, hypnotics, antihistamines, and other pharmaceuticals. Benzophenone exhibits certain carcinogenicity in mouse/rat models under long term exposure. Benzophenone exhibits estrogenic activity. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Benzophenone-d10 | 99.92% | Benzophenone-d10 is the deuterium labeled Benzophenone (HY-Y0546). Benzophenone is an endogenous metabolite. Benzophenone is a photosensitizer, that absorbs UV light, transfers its energy to DNA, and triggers DNA damage. Benzophenone can be used as the fragrance enhancer, ultraviolet curing agent, additive in plastics, or the flavor ingredient. Benzophenone can also be used in the manufacturing of insecticides, agricultural chemicals, hypnotics, antihistamines, and other pharmaceuticals. Benzophenone exhibits certain carcinogenicity in mouse/rat models under long term exposure. Benzophenone exhibits estrogenic activity. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
2,2'-Methylenediphenol-d10 | 90.56% | 2,2'-Methylenediphenol-d10 (2,2'-Dihydroxydiphenylmethane-d10) is the deuterium labeled 2,2'-Methylenediphenol (HY-112034). | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
2-Chloronaphthalene-d7 | 2-Chloronaphthalene-d7 is the deuterium labeled 2-Chloronaphthalene. | |||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
trans-Stilbene-d10 | trans-Stilbene-d10 ((E)-Stilbene-d10) is the deuterium labeled trans-Stilbene (HY-128793). trans-Stilbene ((E)-Stilbene) is used in the manufacturing of dye lasers, optical brighteners, non-steroidal synthetic estrogens. | |||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Benzhydrol (Standard) | ≥98% | Benzhydrol (Standard) is the analytical standard of Benzhydrol. This product is intended for research and analytical applications. Diphenylmethanol is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Diphenylmethanol-d10 | Diphenylmethanol-d10 (Benzhydrol-d10) is the deuterium labeled Benzhydrol (HY-W004059). Diphenylmethanol is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | |||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
4-Chlorobenzophenone (Standard) | ≥98% | 4-Chlorobenzophenone (Standard) is the analytical standard of 4-Chlorobenzophenone. This product is intended for research and analytical applications. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Diphenylmethanimine | 98.55% | Diphenylmethanimine is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
2-Aminobenzophenone | 99.96% | 2-Aminobenzophenone is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
(2-Chlorophenyl)(phenyl)methanone | 98.76% | (2-Chlorophenyl)(phenyl)methanone is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
4-Hydroxybenzophenone | 99.95% | 4‑Hydroxybenzophenone (4HBP) is a major metabolite of Benzophenone (HY-Y0546) and is orally active. 4-Hydroxybenzophenone triggers endoplasmic reticulum stress and activates the PERK-eIF2α-ATF4-CHOP and IRE1α-XBP1s pathways, and inhibits IκB translation. 4-Hydroxybenzophenone induces endoplasmic reticulum stress, unfolded protein response activation, protein homeostasis imbalance, protein aggregation, oxidative stress, ROS accumulation, mitochondrial membrane potential decrease, ATP depletion, and cytotoxicity. 4-Hydroxybenzophenone induces neural stem cell apoptosis (apoptosis) and affects neuronal differentiation. 4-Hydroxybenzophenone promotes malignant proliferation of hepatocellular carcinoma cells and xenograft tumor growth in nude mice. 4-Hydroxybenzophenone can be used in research related to neurodevelopmental toxicity and hepatocellular carcinoma. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
1,2-Diphenylethyne-d10 | 1,2-Diphenylethyne-d10 is the deuterium labeled 1,2-Diphenylethyne. 1,2-Diphenylethyne is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. | |||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
2-Benzoylpyridine (Standard) | ≥98% | 2-Benzoylpyridine (Standard) is the analytical standard of 2-Benzoylpyridine. This product is intended for research and analytical applications. 2-Benzoylpyridine is a biochemical reagent. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
4-Aminobenzophenone | 99.91% | 4-Aminobenzophenone (p-Benzoylaniline; 4-Aminophenyl phenyl ketone; 4-Benzoylaniline) is Benzophenone (HY-Y0546) derivative, which behaves as photosensitizer. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
4,4'-Dihydroxydiphenylmethane-d10 | 99.60% | 4,4'-Dihydroxydiphenylmethane-d10 is a deuterium labeled compound. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
1-Naphthoic acid-d7 | 1-Naphthoic acid-d7 (Naphthalene-1-carboxylic acid-d7) is the deuterium labeled 1-Naphthoic acid (HY-Y0236). Naphthalene-1-carboxylic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | |||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Dibenzylamine-d10 | 98.20% | Dibenzylamine-d10 (Bisbenzylamine-d10) is the deuterium labeled Dibenzylamine. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
2-Phenylacetophenone | 99.91% | 2-Phenylacetophenone has broad-spectrum efflux pump inhibition activity. 2-Phenylacetophenone is a benzoin derivative used as a photoinitiator in vinyl polymerization. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
References
- [1]. EFSA Panel on Food Contact Materials, Enzymes, Flavourings and Processing Aids (CEF); Silano V, et al., Safety of benzophenone to be used as flavouring. EFSA J. 2017 Nov 14;15(11):e05013. [Content Brief]
- [2]. Rhodes MC, et al., Carcinogenesis studies of benzophenone in rats and mice. Food Chem Toxicol. 2007 May;45(5):843-51. [Content Brief]